Indium Phosphite‐Based Porous Solids Exhibiting Organic Sensing and a Facile Route to Superhydrophobicity

In searching for practical crystalline porous solids, two unique hybrid materials with featured functions, In‐bpy and In‐dpe, were prepared without deliberately designed organic linker units or complex post‐modification procedures. Composed of oxalate‐embedded metal phosphite (MPO) sheets and bipyri...

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Veröffentlicht in:Chemistry : a European journal 2018-08, Vol.24 (48), p.12474-12479
Hauptverfasser: Chang, Yu‐Tzu, Lo, Sheng‐Han, Lin, Chia‐Her, Hung, Ling‐I, Wang, Sue‐Lein
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Sprache:eng
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Zusammenfassung:In searching for practical crystalline porous solids, two unique hybrid materials with featured functions, In‐bpy and In‐dpe, were prepared without deliberately designed organic linker units or complex post‐modification procedures. Composed of oxalate‐embedded metal phosphite (MPO) sheets and bipyridyl‐type ligands of varied molecular lengths, they show a common pillar‐layered topology but are the first well‐characterized organo‐MPOs to possess genuine porosity, substantiated by CO2 adsorption, and structural stability under harsh conditions. In‐bpy exhibits a turn‐on fluorescence signal when in contact with p‐xylene, making it the first MPO‐based sensing material with selectivity and recyclability. Furthermore, In‐dpe demonstrates a facile and unprecedented route to the superhydrophobicity of porous solids via a [2+2] photocycloaddition reaction between linker and foreign units. Our findings suggest that MPO may serve as a promising platform for hybrid frameworks to create many more functional porous materials. Two unique hybrid porous materials, In‐bpy and In‐dpe, were demonstrated by adopting Indium phosphite layers as a platform pillared by two distinct bipyridyl‐type ligands. In‐bpy exhibits a sensing ability to p‐xylene with a significant emission enhancement, 20 times the original. The surface wettability of In‐dpe was modified into superhydrophobic by grafting foreign molecules via a photocycloaddition reaction.
ISSN:0947-6539
1521-3765
DOI:10.1002/chem.201802776